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Author/Creator Di Muzio, Antonio

1. Clinical expression of facioscapulohumeral muscular dystrophy in carriers of 1–3 D4Z4 reduced alleles: experience of the FSHD Italian National Registry. Issue 1 (5th January 2016)

Authors:
Nikolic, Ana; Ricci, Giulia; Sera, Francesco; Bucci, Elisabetta; Govi, Monica; Mele, Fabiano; Rossi, Marta; Ruggiero, Lucia; Vercelli, Liliana; Ravaglia, Sabrina; Brisca, Giacomo; Fiorillo, Chiara; Villa, Luisa; Maggi, Lorenzo; Cao, Michelangelo; D'Amico, Maria Chiara; Siciliano, Gabriele; Antoni...
Journal:
BMJ open
Issue:
Volume 6:Issue 1(2016)
Page Start:
Record Type:
Journal Article
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2. Clinical-Genetic Features Influencing Disability in Spastic Paraplegia Type 4: A Cross-sectional Study by the Italian DAISY Network. (30th April 2022)

Authors:
Rossi, Salvatore; Rubegni, Anna; Riso, Vittorio; Barghigiani, Melissa; Bassi, Maria Teresa; Battini, Roberta; Bertini, Enrico; Cereda, Cristina; Cioffi, Ettore; Criscuolo, Chiara; Dal Fabbro, Beatrice; Dato, Clemente; D'Angelo, Maria Grazia; Di Muzio, Antonio; Diamanti, Luca; Dotti, Maria Teresa;...
Journal:
Neurology
Issue:
Volume 8:Number 2(2022)
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Record Type:
Journal Article
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4. Expanding the clinical and genetic spectrum of pathogenic variants in STIM1. Issue 5 (26th August 2021)

Authors:
Ticci, Chiara; Cassandrini, Denise; Rubegni, Anna; Riva, Beatrice; Vattemi, Gaetano; Matà, Sabrina; Ricci, Giulia; Baldacci, Jacopo; Guglielmi, Valeria; Di Muzio, Antonio; Malandrini, Alessandro; Tonin, Paola; Siciliano, Gabriele; Federico, Antonio; Genazzani, Armando A.; Santorelli, Filippo M.; ...
Journal:
Muscle & nerve
Issue:
Volume 64:Issue 5(2021)
Page Start:
567
Record Type:
Journal Article
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